Clinical endocrinology · 2025
Testicular Function After Immune-Checkpoint Inhibitors Treatment.
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Boutros Andrea, Idan Amanda, Sleiman Sue, Bacha Feyrous, Zhang Ting, Jayadev Veena, Menzies Alexander M, Long Georgina V, Handelsman David J
Аннотация
OBJECTIVE: To investigate the effects of immune-checkpoint inhibitors (ICIs) on spermatogenesis and testicular endocrine function in reproductive-age men with melanoma.
DESIGN: Prospective, mixed longitudinal and cross-sectional cohort study.
PATIENTS: Twenty-nine men aged 19-46 years undergoing ICI therapy for melanoma at two Australian centres between 2019 and 2024. Three patients were excluded due to subsequent gonadotoxic therapies. The remaining 26 were evaluable.
MEASUREMENTS: Semen analysis and serum hormone levels (FSH, LH, testosterone) were assessed at baseline and after ICI exposure. Patients with prior cytotoxic chemotherapy or pelvic radiotherapy were excluded.
RESULTS: Among 26 evaluable patients, one man developed persistent azoospermia with marked serum FSH elevation. Overall, median total sperm output per ejaculate declined by 34% (193-127 million per ejaculate) and sperm concentration by 30% (61-43 million/mL), neither statistically significant before or after excluding the case of presumed autoimmune orchitis. On treatment, serum LH and testosterone remained stable while the increase in serum FSH (p = 0.04) was no longer significant after excluding the single man with auto-immune orchitis.
CONCLUSIONS: ICI treatment may be associated with minimal spermatogenic dysfunction, as reflected by modest reductions in sperm output and increased serum FSH levels, despite preserved serum LH and testosterone concentrations, but mostly due to a rare (4% prevalence) case of autoimmune orchitis. The unpredictability of these effects supports routine fertility preservation counselling in young men before ICI initiation.
DESIGN: Prospective, mixed longitudinal and cross-sectional cohort study.
PATIENTS: Twenty-nine men aged 19-46 years undergoing ICI therapy for melanoma at two Australian centres between 2019 and 2024. Three patients were excluded due to subsequent gonadotoxic therapies. The remaining 26 were evaluable.
MEASUREMENTS: Semen analysis and serum hormone levels (FSH, LH, testosterone) were assessed at baseline and after ICI exposure. Patients with prior cytotoxic chemotherapy or pelvic radiotherapy were excluded.
RESULTS: Among 26 evaluable patients, one man developed persistent azoospermia with marked serum FSH elevation. Overall, median total sperm output per ejaculate declined by 34% (193-127 million per ejaculate) and sperm concentration by 30% (61-43 million/mL), neither statistically significant before or after excluding the case of presumed autoimmune orchitis. On treatment, serum LH and testosterone remained stable while the increase in serum FSH (p = 0.04) was no longer significant after excluding the single man with auto-immune orchitis.
CONCLUSIONS: ICI treatment may be associated with minimal spermatogenic dysfunction, as reflected by modest reductions in sperm output and increased serum FSH levels, despite preserved serum LH and testosterone concentrations, but mostly due to a rare (4% prevalence) case of autoimmune orchitis. The unpredictability of these effects supports routine fertility preservation counselling in young men before ICI initiation.